Survival analysis of patients with glioblastoma treated by long-term administration of temozolomide
This analysis aimed to investigate whether the long-term administration of temozolomide (TMZ) claimed a survival advantage for patients with glioblastoma in China.A total of 75 patients with newly diagnosed glioblastoma at the Department of Radiation Oncology, Shenzhen People's Hospital between...
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Veröffentlicht in: | Medicine (Baltimore) 2020-01, Vol.99 (2), p.e18591-e18591 |
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description | This analysis aimed to investigate whether the long-term administration of temozolomide (TMZ) claimed a survival advantage for patients with glioblastoma in China.A total of 75 patients with newly diagnosed glioblastoma at the Department of Radiation Oncology, Shenzhen People's Hospital between August 2008 and August 2016 were retrospectively evaluated during analysis. A propensity-matched analysis was performed to balance the basic characteristics of patients between compared groups. Kaplan-Meier method and Cox proportional hazards model were used to assess progression-free survival (PFS) and overall survival (OS) of patients receiving 6 adjuvant TMZ cycles compared with patients treated with more than 6 cycles.Twenty of 75 patients received more than 6 cycles of TMZ, and the other 55 patients were treated with a median of 6 cycles ranging from 1 to 6. The patients with long-term administration of TMZ had better OS (47.0 months, 95% CI 20.0-73.9 vs 20.6 months, 95% CI 17.9-23.2, P = .014) but not PFS (17.0 months, 95% CI 10.1-24.5 vs 14.2 months, 95% CI 11.8-16.6, P = .133). Balancing the clinical factors with a propensity-matched analysis also showed the significant advantage of prolonged TMZ application in terms of OS but not PFS.Prolonged administration of TMZ beyond 6 cycles did demonstrate survival benefits for patients with initially diagnosed glioblastoma. |
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A propensity-matched analysis was performed to balance the basic characteristics of patients between compared groups. Kaplan-Meier method and Cox proportional hazards model were used to assess progression-free survival (PFS) and overall survival (OS) of patients receiving 6 adjuvant TMZ cycles compared with patients treated with more than 6 cycles.Twenty of 75 patients received more than 6 cycles of TMZ, and the other 55 patients were treated with a median of 6 cycles ranging from 1 to 6. The patients with long-term administration of TMZ had better OS (47.0 months, 95% CI 20.0-73.9 vs 20.6 months, 95% CI 17.9-23.2, P = .014) but not PFS (17.0 months, 95% CI 10.1-24.5 vs 14.2 months, 95% CI 11.8-16.6, P = .133). Balancing the clinical factors with a propensity-matched analysis also showed the significant advantage of prolonged TMZ application in terms of OS but not PFS.Prolonged administration of TMZ beyond 6 cycles did demonstrate survival benefits for patients with initially diagnosed glioblastoma.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000018591</identifier><identifier>PMID: 31914038</identifier><language>eng</language><publisher>United States: the Author(s). Published by Wolters Kluwer Health, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Antineoplastic Agents, Alkylating - administration & dosage ; Antineoplastic Agents, Alkylating - therapeutic use ; Brain Neoplasms - drug therapy ; Brain Neoplasms - mortality ; Brain Neoplasms - therapy ; Chemotherapy, Adjuvant ; Drug Administration Schedule ; Female ; Glioblastoma - drug therapy ; Glioblastoma - mortality ; Glioblastoma - therapy ; Humans ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Neoplasm Grading ; Observational Study ; Propensity Score ; Retrospective Studies ; Temozolomide - administration & dosage ; Temozolomide - therapeutic use ; Young Adult</subject><ispartof>Medicine (Baltimore), 2020-01, Vol.99 (2), p.e18591-e18591</ispartof><rights>the Author(s). Published by Wolters Kluwer Health, Inc.</rights><rights>Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5009-93bf60222869640a881e73b72122eaf342c34a4f8061f742ba3c52525d9e2eff3</citedby><cites>FETCH-LOGICAL-c5009-93bf60222869640a881e73b72122eaf342c34a4f8061f742ba3c52525d9e2eff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959873/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959873/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31914038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quan, Rencui</creatorcontrib><creatorcontrib>Zhang, Huaqing</creatorcontrib><creatorcontrib>Li, Zihuang</creatorcontrib><creatorcontrib>Li, Xianming</creatorcontrib><title>Survival analysis of patients with glioblastoma treated by long-term administration of temozolomide</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>This analysis aimed to investigate whether the long-term administration of temozolomide (TMZ) claimed a survival advantage for patients with glioblastoma in China.A total of 75 patients with newly diagnosed glioblastoma at the Department of Radiation Oncology, Shenzhen People's Hospital between August 2008 and August 2016 were retrospectively evaluated during analysis. A propensity-matched analysis was performed to balance the basic characteristics of patients between compared groups. Kaplan-Meier method and Cox proportional hazards model were used to assess progression-free survival (PFS) and overall survival (OS) of patients receiving 6 adjuvant TMZ cycles compared with patients treated with more than 6 cycles.Twenty of 75 patients received more than 6 cycles of TMZ, and the other 55 patients were treated with a median of 6 cycles ranging from 1 to 6. The patients with long-term administration of TMZ had better OS (47.0 months, 95% CI 20.0-73.9 vs 20.6 months, 95% CI 17.9-23.2, P = .014) but not PFS (17.0 months, 95% CI 10.1-24.5 vs 14.2 months, 95% CI 11.8-16.6, P = .133). Balancing the clinical factors with a propensity-matched analysis also showed the significant advantage of prolonged TMZ application in terms of OS but not PFS.Prolonged administration of TMZ beyond 6 cycles did demonstrate survival benefits for patients with initially diagnosed glioblastoma.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents, Alkylating - administration & dosage</subject><subject>Antineoplastic Agents, Alkylating - therapeutic use</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - mortality</subject><subject>Brain Neoplasms - therapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Glioblastoma - drug therapy</subject><subject>Glioblastoma - mortality</subject><subject>Glioblastoma - therapy</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Observational Study</subject><subject>Propensity Score</subject><subject>Retrospective Studies</subject><subject>Temozolomide - administration & dosage</subject><subject>Temozolomide - therapeutic use</subject><subject>Young Adult</subject><issn>0025-7974</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkN1OGzEQha2KqgTaJ6hU-QU29d-u1zeVEH9FAnEBvbZmd-3E4F1HtpMoPH1N01JgfDHS-Jxv7IPQV0rmlCj5_eZsTv4XbWtFP6AZrXlT1aoRB2hGCKsrqaQ4REcpPRQRl0x8QoecKioIb2eov1vHjduAxzCB3yWXcLB4BdmZKSe8dXmJF96FzkPKYQSco4FsBtztsA_TosomjhiG0U0u5Vh8YXomZDOGp-DD6AbzGX204JP58rcfo18X5_enP6vr28ur05Prqq8JUZXinW0IY6xtyvMJtC01kneSUcYMWC5YzwUI25KGWilYB7yvWTmDMsxYy4_Rjz13te5GM_TlBxG8XkU3QtzpAE6_vZncUi_CRjeqVq3kBcD3gD6GlKKxL15K9HPm-uZMv8-8uL69Xvvi-RdyEYi9YBt8iSs9-vXWRL004PPyD6-WilWMsIKkhFRlwhT_DSn-juQ</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Quan, Rencui</creator><creator>Zhang, Huaqing</creator><creator>Li, Zihuang</creator><creator>Li, Xianming</creator><general>the Author(s). Published by Wolters Kluwer Health, Inc</general><general>Wolters Kluwer Health</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20200101</creationdate><title>Survival analysis of patients with glioblastoma treated by long-term administration of temozolomide</title><author>Quan, Rencui ; Zhang, Huaqing ; Li, Zihuang ; Li, Xianming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5009-93bf60222869640a881e73b72122eaf342c34a4f8061f742ba3c52525d9e2eff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents, Alkylating - administration & dosage</topic><topic>Antineoplastic Agents, Alkylating - therapeutic use</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - mortality</topic><topic>Brain Neoplasms - therapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Glioblastoma - drug therapy</topic><topic>Glioblastoma - mortality</topic><topic>Glioblastoma - therapy</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Observational Study</topic><topic>Propensity Score</topic><topic>Retrospective Studies</topic><topic>Temozolomide - administration & dosage</topic><topic>Temozolomide - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quan, Rencui</creatorcontrib><creatorcontrib>Zhang, Huaqing</creatorcontrib><creatorcontrib>Li, Zihuang</creatorcontrib><creatorcontrib>Li, Xianming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quan, Rencui</au><au>Zhang, Huaqing</au><au>Li, Zihuang</au><au>Li, Xianming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Survival analysis of patients with glioblastoma treated by long-term administration of temozolomide</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>99</volume><issue>2</issue><spage>e18591</spage><epage>e18591</epage><pages>e18591-e18591</pages><issn>0025-7974</issn><eissn>1536-5964</eissn><abstract>This analysis aimed to investigate whether the long-term administration of temozolomide (TMZ) claimed a survival advantage for patients with glioblastoma in China.A total of 75 patients with newly diagnosed glioblastoma at the Department of Radiation Oncology, Shenzhen People's Hospital between August 2008 and August 2016 were retrospectively evaluated during analysis. A propensity-matched analysis was performed to balance the basic characteristics of patients between compared groups. Kaplan-Meier method and Cox proportional hazards model were used to assess progression-free survival (PFS) and overall survival (OS) of patients receiving 6 adjuvant TMZ cycles compared with patients treated with more than 6 cycles.Twenty of 75 patients received more than 6 cycles of TMZ, and the other 55 patients were treated with a median of 6 cycles ranging from 1 to 6. The patients with long-term administration of TMZ had better OS (47.0 months, 95% CI 20.0-73.9 vs 20.6 months, 95% CI 17.9-23.2, P = .014) but not PFS (17.0 months, 95% CI 10.1-24.5 vs 14.2 months, 95% CI 11.8-16.6, P = .133). Balancing the clinical factors with a propensity-matched analysis also showed the significant advantage of prolonged TMZ application in terms of OS but not PFS.Prolonged administration of TMZ beyond 6 cycles did demonstrate survival benefits for patients with initially diagnosed glioblastoma.</abstract><cop>United States</cop><pub>the Author(s). Published by Wolters Kluwer Health, Inc</pub><pmid>31914038</pmid><doi>10.1097/MD.0000000000018591</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Antineoplastic Agents, Alkylating - administration & dosage Antineoplastic Agents, Alkylating - therapeutic use Brain Neoplasms - drug therapy Brain Neoplasms - mortality Brain Neoplasms - therapy Chemotherapy, Adjuvant Drug Administration Schedule Female Glioblastoma - drug therapy Glioblastoma - mortality Glioblastoma - therapy Humans Kaplan-Meier Estimate Male Middle Aged Neoplasm Grading Observational Study Propensity Score Retrospective Studies Temozolomide - administration & dosage Temozolomide - therapeutic use Young Adult |
title | Survival analysis of patients with glioblastoma treated by long-term administration of temozolomide |
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